تفاعل #75436

ord-74d13327b7ce47cb8e1cfe09732eb00d

معادلة التفاعل

O
Water
CC(C)(CN)CN
2,2-dimethyl-1,3-propane diamine
CC(N=O)C(C)(C)Cl
3-chloro-3-methyl-2-nitrosobutane
CO
methanol
CCC(=NO)C(C)(C)NCC(C)(C)CN
compound
CCC(=NO)C(C)(C)NCC(C)(C)CN
N-(3-Amino-2,2-dimethylpropyl)-1-amino-1,1-dimethyl-2-butanone Oxime

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe solvent was removed under reduced pressure
  2. 2
    أخرىto give a paste
  3. 3
    درجة الحرارةthe solution was cooled in an ice bath
  4. 4
    ترشيحThe solution was filtered
  5. 5
    workup.ADDITIONthe filtrate was adjusted to pH 10-11 by the addition of sodium hydroxide
  6. 6
    درجة الحرارةThe solution was cooled again
  7. 7
    ترشيحfiltered
  8. 8
    تركيزThe filtrate was concentrated under reduced pressure to a paste
  9. 9
    استخلاصextracted with ether repeatedly (10×50 mL)
  10. 10
    تركيزThe combined ether solution was concentrated
  11. 11
    أخرىto give an oil which
  12. 12
    أخرىwas recrystallized twice from petroleum ether

الإجراء التجريبي

To a solution of 2,2-dimethyl-1,3-propane diamine (69 g, 0.75 mole) in dry methanol (100 mL), 3-chloro-3-methyl-2-nitrosobutane (20.55 g, 0.15 mole, Example 1) was added in portions at 0° C. over a period of 2 hours. The reaction mixture was then stirred at room temperature for 20 hours. The solvent was removed under reduced pressure to give a paste. Water (50 mL) was added, and the solution was cooled in an ice bath. The solution was filtered and the filtrate was adjusted to pH 10-11 by the addition of sodium hydroxide. The solution was cooled again and filtered. The filtrate was concentrated under reduced pressure to a paste and then extracted with ether repeatedly (10×50 mL). The combined ether solution was concentrated to give an oil which was recrystallized twice from petroleum ether to yield the title A compound as a colorless crystalline solid (20.0 g), m.p. 58-60° C. 1H NMR [CDCl3]: δ0.85 (s, 6H, C—Me2), 1.28 (s, 6H, N—CMe2), 1.9 (s, 3H, N═CMe), 2.2 (s, 2H, NCH2) and 2.6 (s, 2H, N—CH2).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06699458B2uspto-grants-2004_03